一名来自卡塔尔的女孩因潜水损伤导致婴儿期后获得性脑瘫:罕见病因和治疗挑战。

Aamir Jalal Al-Mosawi
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摘要

背景:脑瘫是一种异质性疾病,可导致终身残疾,并伴有非进行性脑损伤。它通常是由产前、围产期、产后早期和新生儿疾病引起的。然而,新生儿后获得性脑瘫病例也有报道,通常是由感染引起的。患者和方法:一位来自卡塔尔的女孩因淹水损伤导致严重脑瘫,她的家人向我们咨询了可能的治疗方法。本文对临床表现和脑成像异常进行了描述,并对相关文献进行了回顾,目的是提出可能的循证治疗方法。结果:在23个月大时,一名先前健康的女孩在经历了浸没损伤后发生了缺氧性脑病。MRI显示明显的缺氧缺血性损伤,主要影响深部灰质、海马、中脑和后皮层。脑电图显示脑活动弥漫性缓慢,背景弥漫性减弱,未见癫痫异常,提示弥漫性皮质损伤所致弥漫性脑病。在大约三岁半的时候,她的家人向我们咨询了她的情况,因为她仍然对环境没有任何意识,没有明显的自发运动。她的头部控制不好。不能单独坐或站立,并且有弯曲的姿势。她每天服用左乙拉西坦(Keppra)、安定和巴氯芬30毫克。她仍在进行气管切开术,并通过胃造口管进食。结论:本文描述了婴儿后重度脑瘫的罕见发生情况。重点是在脑瘫中应用循证多因素治疗的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Girl from Qatar with Post-Infantile Acquired Cerebral Palsy Caused By Submersion Injury: A Rare Etiology and a Therapeutic-Challenge.
Background: Cerebral palsy is a heterogeneous disorder that can cause a lifelong disability that is associated with a non-progressive damage in the brain. It is commonly caused by antenatal, perinatal, early postnatal and neonatal conditions. However, post-neonatal cases of acquired cerebral palsy have also been reported, and were commonly caused by infection. Patients and Methods: The family of a girl from Qatar, who developed severe cerebral palsy caused by submersion injury, consulted us about the possible therapies for her condition. Clinical picture and brain imaging abnormalities are described, and the relevant literatures were reviewed with the aim of suggesting possible evidence-based therapies. Results: At the age of 23 months, a previously healthy girl developed anoxic encephalopathy after experiencing submersion injury. MRI showed evidence of significant hypoxic ischemic injury primarily affecting the deep grey matter, hippocami, mid-brain and the posterior cortex. EEG showed diffuse slowness of cerebral activity and diffuse attenuation of the background without no epileptic abnormalities suggesting diffuse encephalopathy resulting from diffuse cortical injury. At the about age of three and half years, her family consulted us about her condition as she was still showing no awareness to the environment, showing no significant spontaneous movements. She had poor head control. Unable to sit or stand alone, and had a flexed posture. She was on levetiracetam (Keppra), diazepam, and baclofen 30 mg daily. She was still having tracheotomy, and was fed through gastrostomy tube. Conclusion: In this paper, the rare occurrence of severe post-infantile cerebral palsy is described. Emphasis is made on the possibility of using evidence-based multi-factorial therapies in cerebral palsy.
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